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首页> 外文期刊>American Journal of Translational Research >MicroRNA-146b-3p regulates the development and progression of cerebral infarction with diabetes through RAF1/P38MAPK/COX-2 signaling pathway
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MicroRNA-146b-3p regulates the development and progression of cerebral infarction with diabetes through RAF1/P38MAPK/COX-2 signaling pathway

机译:MicroRNA-146b-3p通过RAF1 / P38MAPK / COX-2信号通路调节糖尿病性脑梗死的发生和发展

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摘要

Diabetes has been considered as an independent risk factor for cerebral infarction. However, the pathological mechanism of cerebral infarction with diabetes (DMCI) is still rarely known. In this study, we try to explore the relationship between microRNA-146b-3p (miR-146b-3p) and DMCI patients. The peripheral blood mononuclear cells were separated after the patients were selected from our hospital. Firstly, the content of IL-6 and COX-2 was detected by ELISA. Then, the total RNAs were extracted and analyzed by microRNA (miRNA) microarray. Moreover, the target genes of miR-146b-3p were predicted by online miRNA target prediction algorithms. Meanwhile, luciferase reporter system was used for assaying the target gene for miRNA-146b-3p. Simultaneously, RT-PCR assay was used for the miRNA expression detection. Furthermore, western blot was applied to determine the expression of the signal pathway involved proteins. Our results demonstrated that expression of IL-6 and COX-2 were remarkably up-regulated in peripheral blood of DMCI patients compared with that in normal control group. In addition, miRNA microarray data suggested that miR-146b-3p expression was significantly down-regulated in DMCI patients, with v-raf-1 expression negatively regulated. Moreover, miR-146b-3p regulated RAF1 expression was found to mediate P38MAPK signaling activation in thrombosis patients. The following research indicated that activation of RAF1 trough miR-146b-3p down-regulation contributed to activation of RAF/P38MAPK/COX-2 signaling pathway in vascular infarction. Our data have implied that altered expression of miR-146b-3p is closely related to the progression and development of DCMI mediating the RAF/P38MAPK/COX-2 signal transduction pathway.
机译:糖尿病被认为是脑梗死的独立危险因素。然而,糖尿病性脑梗死的病理机制仍然鲜为人知。在这项研究中,我们尝试探索microRNA-146b-3p(miR-146b-3p)与DMCI患者之间的关系。从我院选择患者后,分离外周血单个核细胞。首先,通过ELISA检测IL-6和COX-2的含量。然后,提取总RNA,并通过microRNA(miRNA)微阵列分析。此外,通过在线miRNA靶标预测算法预测了miR-146b-3p的靶基因。同时,使用萤光素酶报告系统分析miRNA-146b-3p的靶基因。同时,将RT-PCR测定用于miRNA表达检测。此外,采用蛋白质印迹法来确定信号途径所涉及蛋白的表达。我们的结果表明,与正常对照组相比,DMCI患者外周血中IL-6和COX-2的表达明显上调。此外,miRNA基因芯片数据表明,在DMCI患者中,miR-146b-3p的表达明显下调,而v-raf-1的表达则呈负调控。此外,发现在血栓形成患者中,miR-146b-3p调节的RAF1表达介导P38MAPK信号激活。以下研究表明,RAF1槽miR-146b-3p下调的激活有助于血管梗塞中RAF / P38MAPK / COX-2信号通路的激活。我们的数据表明,miR-146b-3p表达的改变与DCMI介导RAF / P38MAPK / COX-2信号转导通路的进展和发展密切相关。

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